RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:In situ targeting nanoparticles-hydrogel hybrid system for combined chemo-immunotherapy of glioma.
In situ targeting nanoparticles-hydrogel hybrid system for combined chemo-immunotherapy of glioma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
众所周知,胶质瘤是目前最恶性的脑肿瘤。由于血脑屏障(BBB)和肿瘤细胞异质性的存在,全身化疗对胶质瘤手术切除后的治疗效果不理想,甚至可能损害机体免疫系统。
在此,我们开发了一种原位缓释水凝胶递送系统,通过将化疗药物和免疫佐剂经切除腔局部递送,用于胶质瘤的化疗-免疫联合治疗。简言之,我们将胶质瘤归巢肽修饰的紫杉醇靶向纳米粒(PNP PTX)和甘露糖化免疫佐剂CpG靶向纳米粒(MNP CpG)嵌入PLGA 1750 -PEG 1500 -PLGA 1750 热敏水凝胶骨架中(PNP PTX &MNP CpG @Gel)。体外和体内结果表明,该靶向纳米粒-水凝胶杂化系统在注射到胶质瘤切除腔后可交联形成凝胶药物储库。随后,缓释的PNP PTX可靶向残留浸润的胶质瘤细胞并产生肿瘤抗原。
同时,MNP CpG靶向并激活抗原呈递细胞,增强肿瘤抗原呈递能力,并激活CD8 + T和NK细胞以逆转胶质瘤微环境的免疫抑制。
本研究表明,PNP PTX &MNP CpG @Gel系统可通过化疗-免疫治疗增强胶质瘤的治疗效果。
It is well known that glioma is currently the most malignant brain tumor. Because of the existence of blood-brain barrier (BBB) and tumor cell heterogeneity, systemic chemotherapy exerts unsatisfied therapeutic effect for the treatment of glioma after surgical resection and may even damage the body's immune system.
Here, we developed an in situ sustained-release hydrogel delivery system for combined chemo-immunotherapy of glioma by combined chemotherapy drug and immunoadjuvant through the resection cavity local delivery. Briefly, glioma homing peptide modified paclitaxel targeting nanoparticles (PNP PTX ) and mannitolated immunoadjuvant CpG targeting nanoparticles (MNP CpG ) were embedded into PLGA 1750 -PEG 1500 -PLGA 1750 thermosensitive hydrogel framework (PNP PTX &MNP CpG @Gel).
The in vitro and in vivo results showed that the targeting nanoparticles-hydrogel hybrid system could cross-link into a gel drug reservoir when injected into the resection cavity of glioma. And then, the sustained-release PNP PTX could target the residual infiltration glioma cells and produce tumor antigens. Meanwhile, MNP CpG targeted and activated the antigen-presenting cells, which enhanced the tumor antigen presentation ability and activated CD8 + T and NK cells to reverse immunosuppression of glioma microenvironment.
This study indicated that the PNP PTX &MNP CpG @Gel system could enhance the therapeutic effect of glioma by chemo-immunotherapy.
MEMBER ACCOUNT
登录成功会直接打开下一页。